Identity
- Trade Name
- Modpod FDA UDI
- Generic Name
- Static/intermittent powered traction system, mobile FDA UDI
- Device Name
- Modpod brand powered, static/intermittent, mobile traction system FDA UDI
- Model / Reference
- 12.1000 FDA UDI
- Description
- Modpod brand powered, static/intermittent, mobile traction system FDA UDI
Identifiers
- Catalog Number
- 12.1000 FDA UDI
- Primary DI / UDI-DI
- 00853096004151 FDA UDI
- 510(k) Number
- K150695 FDA UDI
- FDA Product Code
- ITH FDA UDI
- GMDN Term
- Static/intermittent powered traction system, mobile FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5900 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Width — 39.4 Centimeter FDA UDILength — 76.8 Centimeter FDA UDIHeight — 27.9 Centimeter FDA UDI
Modpod by Hollywog, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Hollywog, LLC
Sources (1)
- FDA UDI d01f5ea8-a60f-49c7-a33a-195ca1d48268 39 fields · synced May 31, 2026